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Nature Genetics|September 7, 2001
Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic diseaseT J MacDonald, K M Brown, B LaFleur, et al.Muscle & Nerve|December 18, 2001
Severe autosomal recessive rippling muscle diseaseR L Koul, R P Chand, A Chacko, et al.The Journal of Endocrinology|September 1, 1994
Tissue-specific regulation of the growth hormone receptor gene in streptozocin-induced diabetes in the ratR K Menon, D A Stephan, R H Rao, et al.Molecular Psychiatry|May 3, 2002
No missense mutation of WKL1 in a subgroup of probands with schizophreniaJ M Devaney, E A Donarum, K M Brown, et al.Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15A H Chen, D A Stephan, T Hasson, et al.Circulation|February 7, 2001
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardiaP J Laitinen, K M Brown, K Piippo, et al.Neurology|October 10, 2008
Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1D S Stamm, C M Powell, J M Stajich, et al.Human Molecular Genetics|February 13, 2001
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)N Tiso, D A Stephan, A Nava, et al.Molecular Psychiatry|December 21, 2006
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14D Q Ma, M L Cuccaro, J M Jaworski, et al.Molecular Genetics and Metabolism|June 2, 2000
Positional cloning utilizing genomic DNA microarrays: the Niemann-Pick type C gene as a model systemD A Stephan, Y Chen, Y Jiang, et al.Pageof 3